Metal-support
interactions can significantly affect the catalytic
performance of heterogeneous catalysts and have been studied extensively
in thermal catalysis and electrocatalysis. However, the role of strong
metal-support interactions (SMSIs) in regulating photoinduced electron
transfer has been rarely investigated in photocatalysis. In this study,
we have prepared two model catalysts using the impregnation methodone
with SMSI effect (Ru/CeO2) and the other with suppressed
SMSI effect (Ru/CeO2–H2)and tested
them for photothermal CO2 methanation. The methane production
rate of Ru/CeO2–H2 (275.1 mmol/gRu/h) was more than twice that of Ru/CeO2 (111.2
mmol/gRu/h) at 200 °C under light irradiation. Various
characterizations and theoretical calculations suggest that hot electrons,
generated by local surface plasma, transferred to the Ru/CeO2–H2 from the dispersed Ru sites, filling the oxygen
vacancies in Ru/CeO2–H2, where the adsorption
and activation of CO2 was enhanced under light irradiation.
Also, it is evident that the electron-deficient Ru sites speed up
the decomposition of H2. The in situ diffuse
reflectance infrared Fourier transform spectroscopy (DRIFTS) studies
showed that CO2 methanation on Ru/CeO2–H2 and Ru/CeO2 chiefly followed the formate-intermediated
pathway, although the CO-intermediated pathway was also present. This
study offers a technique to enhance photothermal CO2 methanation
by controlling the interaction between the metal and the support.